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直接对蚊虫提取物中的甲病毒进行广泛检测。

Direct broad-range detection of alphaviruses in mosquito extracts.

作者信息

Eshoo Mark W, Whitehouse Chris A, Zoll Scott T, Massire Christian, Pennella Thuy-Trang D, Blyn Lawrence B, Sampath Rangarajan, Hall Thomas A, Ecker Joseph A, Desai Anjali, Wasieloski Leonard P, Li Feng, Turell Michael J, Schink Amy, Rudnick Karl, Otero Glen, Weaver Scott C, Ludwig George V, Hofstadler Steven A, Ecker David J

机构信息

Ibis Biosciences, 1891 Rutherford Rd., Carlsbad, CA 92008, USA.

出版信息

Virology. 2007 Nov 25;368(2):286-95. doi: 10.1016/j.virol.2007.06.016. Epub 2007 Jul 25.

Abstract

Members of the genus Alphavirus are a diverse group of principally mosquito-borne RNA viruses. There are at least 29 species and many more subtypes of alphaviruses and some are considered potential bioweapons. We have developed a multi-locus RT-PCR followed by electrospray ionization mass spectrometry (RT-PCR/ESI-MS) assay that uses the amplicon base compositions to detect and identify alphaviruses. A small set of primer pairs targeting conserved sites in the alphavirus RNA genome were used to amplify a panel of 36 virus isolates representing characterized Old World and New World alphaviruses. Base compositions from the resulting amplicons could be used to unambiguously determine the species or subtype of 35 of the 36 isolates. The assay detected, without culture, Venezuelan equine encephalitis virus (VEEV), Eastern equine encephalitis virus (EEEV), and mixtures of both in pools consisting of laboratory-infected and -uninfected mosquitoes. Further, the assay was used to detect alphaviruses in naturally occurring mosquito vectors collected from locations in South America and Asia. Mosquito pools collected near Iquitos, Peru, were found to contain an alphavirus with a very distinct signature. Subsequent sequence analysis confirmed that the virus was a member of the Mucambo virus species (subtype IIID in the VEEV complex). The assay we have developed provides a rapid, accurate, and high-throughput assay for surveillance of alphaviruses.

摘要

甲病毒属的成员是一类主要由蚊子传播的多样的RNA病毒。甲病毒至少有29个种以及更多的亚型,其中一些被认为是潜在的生物武器。我们开发了一种多位点逆转录聚合酶链反应(RT-PCR)结合电喷雾电离质谱(RT-PCR/ESI-MS)的检测方法,该方法利用扩增子的碱基组成来检测和鉴定甲病毒。使用一小组靶向甲病毒RNA基因组保守位点的引物对,扩增了一组36种病毒分离株,这些分离株代表了已鉴定的旧世界和新世界甲病毒。所得扩增子的碱基组成可用于明确确定36种分离株中35种的种或亚型。该检测方法无需培养即可检测委内瑞拉马脑炎病毒(VEEV)、东部马脑炎病毒(EEEV)以及由实验室感染和未感染蚊子组成的混合样本中的这两种病毒。此外,该检测方法还用于检测从南美和亚洲各地采集的自然存在的蚊子媒介中的甲病毒。在秘鲁伊基托斯附近采集的蚊子样本中发现含有一种具有非常独特特征的甲病毒。随后的序列分析证实该病毒是穆坎博病毒种的一个成员(在VEEV复合体中为IIID亚型)。我们开发的这种检测方法为甲病毒监测提供了一种快速、准确且高通量的检测方法。

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